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dc.contributor.authorKillip, M. J.
dc.contributor.authorYoung, D. F.
dc.contributor.authorPrecious, B. L.
dc.contributor.authorGoodbourn, S.
dc.contributor.authorRandall, R. E.
dc.date.accessioned2012-03-16T13:01:05Z
dc.date.available2012-03-16T13:01:05Z
dc.date.issued2012-02
dc.identifier17784158
dc.identifierc94179de-4b4f-4506-bf2c-979a152cdc3c
dc.identifier000300139500009
dc.identifier84855945567
dc.identifier.citationKillip , M J , Young , D F , Precious , B L , Goodbourn , S & Randall , R E 2012 , ' Activation of the beta interferon promoter by paramyxoviruses in the absence of virus protein synthesis ' , Journal of General Virology , vol. 93 , no. 2 , pp. 299-307 . https://doi.org/10.1099/vir.0.037531-0en
dc.identifier.issn0022-1317
dc.identifier.otherORCID: /0000-0002-9304-6678/work/60427038
dc.identifier.urihttps://hdl.handle.net/10023/2451
dc.description.abstractConflicting reports exist regarding the requirement for virus replication in interferon (IFN) induction by paramyxoviruses. Our previous work has demonstrated that pathogen-associated molecular patterns capable of activating the IFN-induction cascade are not normally generated during virus replication, but are associated instead with the presence of defective interfering (DI) viruses. We demonstrate here that DIs of paramyxoviruses, including parainfluenza virus 5, mumps virus and Sendai virus, can activate the IFN-induction cascade and the IFN-beta promoter in the absence of virus protein synthesis. As virus protein synthesis is an absolute requirement for paramyxovirus genome replication, our results indicate that these DI viruses do not require replication to activate the IFN-induction cascade.
dc.format.extent9
dc.format.extent1218305
dc.language.isoeng
dc.relation.ispartofJournal of General Virologyen
dc.subjectQR355 Virologyen
dc.subject.lccQR355en
dc.titleActivation of the beta interferon promoter by paramyxoviruses in the absence of virus protein synthesisen
dc.typeJournal articleen
dc.contributor.sponsorThe Wellcome Trusten
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1099/vir.0.037531-0
dc.description.statusPeer revieweden
dc.identifier.grantnumber087751/A/08/Zen


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